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Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients — Treatment Landscape & Competitive Intelligence

Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients (disease) competitive landscape: 3 marketed treatments tracked, 0 Phase 3 candidates, 0 Phase 2 candidates. Recent regulatory actions and upcoming PDUFA dates across the entire treatment set.

3 marketed 0 Phase 3 0 Phase 2 Live · 30-min refresh

Marketed treatment landscape

Approved drugs treating Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients, deduplicated by molecule. See the full disease page for line-of-therapy detail.

DrugGenericSponsorClassTargetLine of therapyFirst approval
Vistide CIDOFOVIR Gilead Sciences cidofovir 1996-01-01
Foscavir FOSCARNET Clinigen Hlthcare Pyrophosphate Analog DNA Polymerase Inhibitor 1991-01-01
Vistide Vistide Gustave Roussy, Cancer Campus, Grand Paris DNA polymerase catalytic subunit

Phase 3 pipeline

No Phase 3 pipeline candidates tracked.

Phase 2 pipeline

No Phase 2 pipeline candidates tracked.

Recent regulatory actions (last 90 days)

No regulatory actions in the last 90 days for this treatment set.

Upcoming PDUFA dates (next 180 days)

No PDUFA dates in the next 180 days for this treatment set.

Sponsor landscape

  1. Clinigen Hlthcare · 1 drug in Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients
  2. Gilead Sciences · 1 drug in Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients
  3. Gustave Roussy, Cancer Campus, Grand Paris · 1 drug in Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients

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Every new regulatory action, PDUFA date, or trial completion in Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients:

Cite this brief

Drug Landscape (2026). Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients — Treatment Landscape & Competitive Intelligence Brief. https://druglandscape.com/ci/disease/acyclovir-resistant-mucocutaneous-hsv-in-immunocompromised-patients. Accessed 2026-06-10.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing